JPWO2017203636A1 - Liquid delivery device, treatment device unit, and treatment system - Google Patents

Abstract

A liquid delivery device for a treatment instrument that is used by being attached to a grasping portion of a treatment instrument capable of grasping a living tissue includes a port that receives a fluid, and a grasping surface that can grasp the living tissue among the grasping portions. And a cover for covering the back surface on the opposite side. The cover cooperates with the grip portion to form a continuous channel from the port, and allows the liquid received from the port to flow out between the edge of the cover adjacent to the grip surface and the edge of the grip surface.

Description

  The present invention relates to a liquid delivery tool for a treatment instrument used with a treatment instrument, a treatment instrument unit having a liquid delivery instrument, and a treatment system.

For example, US 2007/0049920 A1 discloses a treatment tool capable of performing treatment such as coagulation by raising the temperature of a living tissue treatment target to a temperature exceeding the temperature at which the protein denatures using high-frequency energy. ing. When high-frequency energy is used to denature proteins, the living tissue to be treated may become high temperature that is carbonized or sticks to the electrode.
Even when a treatment target of a biological tissue is treated using high-frequency energy while a liquid such as physiological saline is dropped on the treatment target of the biological tissue, the protein to be treated can be denatured. On the other hand, it has been found that in such a treatment, it is possible to avoid a rise in temperature at which the treatment target is carbonized by dripping the liquid onto the treatment target. In addition, it has been found that in such treatment, it is suppressed that the biological tissue to be treated adheres to the electrode due to the dripping of the liquid onto the treatment subject.

  When a liquid such as physiological saline is to be dripped onto a treatment target, the treatment tool disclosed in US 2007/0049920 A1 may cause the liquid such as physiological saline to flow to an unintended position away from the treatment target. In this case, energy may be used at a position away from the treatment target, and it becomes difficult to efficiently apply the energy to a desired position (treatment target).

  The present invention is used together with a treatment tool, and a treatment tool unit having a liquid delivery tool for a treatment tool and a treatment tool unit that can efficiently treat a treatment target while allowing a liquid such as physiological saline to flow out to the treatment target of a living tissue. And it aims at providing a treatment system.

  According to one aspect of the present invention, a liquid delivery device for a treatment instrument that is used by being attached to a grasping portion of a treatment instrument capable of grasping a living tissue includes a port that receives a fluid, a port that receives a fluid, Among them, a cover that covers the back surface on the opposite side to the gripping surface capable of gripping the living tissue, forms a flow path continuous from the port in cooperation with the gripping portion, and receives the liquid received from the port The cover has a cover that flows out from between the edge of the cover adjacent to the gripping surface and the edge of the gripping surface.

FIG. 1 is a schematic view showing a treatment system according to the first to sixth embodiments. FIG. 2A is a schematic cross-sectional view illustrating a state in which the liquid feeding device of the suction / liquid feeding unit is to be attached to the first grip portion of the end effector of the treatment device of the treatment system according to the first embodiment. 2B is a schematic partial cross-sectional view showing a state in which the liquid feeding tool of the suction / liquid feeding unit of the treatment system according to the first embodiment is viewed from a position along line 2B-2B in FIG. 2A. 2C is a cross-sectional view taken along line 2C-2C in FIG. 2A of the liquid delivery tool of the suction / liquid delivery unit of the treatment system according to the first embodiment. FIG. 3A is a schematic diagram showing a state in which the treatment instrument unit is configured by mounting the liquid delivery tool of the suction / liquid delivery unit on the first grip portion of the end effector of the treatment instrument of the treatment system according to the first embodiment. It is sectional drawing. FIG. 3B shows a state in which the treatment instrument unit is configured by attaching the liquid delivery tool of the suction / liquid delivery unit to the first grip portion of the end effector of the treatment instrument of the treatment system according to the first embodiment. It is the schematic seen from the position which follows a 3B-3B line. FIG. 3C shows a state in which the liquid feeding device of the suction / liquid feeding unit is attached to the first grip portion of the end effector of the treatment device of the treatment system according to the first embodiment, along the line 3C-3C in FIGS. 3A and 3B. It is the schematic seen from the position which follows. FIG. 4 is a schematic perspective view showing a state in which the treatment instrument unit is configured by attaching the suction / liquid feeding unit to the first grip portion of the treatment instrument of the treatment system according to the first embodiment. FIG. 5 is a schematic perspective view showing the vicinity of the distal end portion of the tube unit of the suction / liquid feeding unit of the treatment system according to the first embodiment. 6A is a schematic view of the tube body of the tube unit of the suction / liquid feeding unit of the treatment system according to the first embodiment as viewed from the position along the line 6A-6A in FIG. 6B is a schematic view showing a state where a shaft is inserted through the tube main body of the tube unit shown in FIG. 6A. FIG. 7A is a schematic view showing a state in which the fixed arm of the connecting portion of the tube unit of the suction / liquid feeding unit of the treatment system according to the first embodiment is about to be fitted into the recess of the rotary knob of the treatment tool. FIG. 7B is a schematic diagram showing a state in which the treatment tool unit is configured by fitting the fixed arm of the connection portion of the tube unit of the suction / liquid feeding unit of the treatment system according to the first embodiment to the recess of the rotary knob of the treatment tool. FIG. FIG. 8A is a schematic view in the connecting portion showing a state where the shaft is inserted into the tube main body and the connecting portion of the tube unit of the suction / liquid feeding unit of the treatment system according to the first embodiment. FIG. 8B is a schematic view of the tube main body and the connecting portion in FIG. 8A of the tube unit of the suction / liquid feeding unit of the treatment system according to the first embodiment, as viewed from the position along line 8B-8B. 9 shows a state where the shaft is inserted through the tube main body of the tube unit shown in FIG. 6A, and negative pressure is applied to the tube unit of the suction / liquid feeding unit of the treatment system according to the first embodiment. It is the schematic which shows the state which forms a space in the position adjacent to each protrusion, when a surface is made to adjoin or closely_contact | adhere to the outer peripheral surface of a shaft. FIG. 10 is a schematic view showing a state in which the liquid feeding unit is attached to the treatment instrument according to a modification of the first embodiment, in which the first and second gripping portions are relatively movable, and the outer peripheral surface of the shaft It is the schematic which shows the state which made various treatment devices penetrate the lumen between the inner peripheral surfaces of a tube. FIG. 11A is a schematic cross-sectional view illustrating a state in which the liquid feeding tool of the suction / liquid feeding unit is to be attached to the first grip portion of the end effector of the treatment tool of the treatment system according to the second embodiment. FIG. 11B is a schematic partial cross-sectional view showing a state in which the liquid feeding tool of the suction / liquid feeding unit of the treatment system according to the second embodiment is viewed from the position along the line 11B-11B in FIG. 11A. FIG. 11C is a cross-sectional view taken along line 11C-11C in FIG. 11A of the liquid delivery tool of the suction / liquid delivery unit of the treatment system according to the second embodiment. FIG. 12A is a schematic diagram showing a state in which the treatment instrument unit is configured by mounting the liquid delivery tool of the suction / liquid delivery unit to the first grip portion of the end effector of the treatment instrument of the treatment system according to the second embodiment. It is sectional drawing. FIG. 12B shows a state in which the treatment instrument unit is configured by attaching the liquid delivery tool of the suction / liquid delivery unit to the first grip portion of the end effector of the treatment instrument of the treatment system according to the second embodiment. It is the schematic seen from the position which follows a 12B-12B line. 12C shows a state in which the liquid feeding device of the suction / liquid feeding unit is attached to the first grip portion of the end effector of the treatment device of the treatment system according to the second embodiment, along the line 12C-12C in FIGS. 12A and 12B. It is the schematic seen from the position which follows. FIG. 13 is a schematic diagram showing a state in which the treatment instrument unit is configured by mounting the liquid delivery tool of the suction / liquid delivery unit to the first grip portion of the end effector of the treatment instrument of the treatment system according to the third embodiment. It is sectional drawing. FIG. 14A is a schematic view of the tube body of the tube unit of the suction / liquid feeding unit of the treatment system according to the fourth embodiment as viewed from the position along line 6A-6A in FIG. 14B is a schematic view showing a state where a shaft is inserted through the tube main body of the tube unit shown in FIG. 14A. FIG. 15A is a schematic view of the tube body of the tube unit of the suction / liquid feeding unit of the treatment system according to the fifth embodiment as viewed from the position along line 6A-6A in FIG. FIG. 15B is a schematic view showing a state where a shaft is inserted through the tube main body of the tube unit shown in FIG. 15A. FIG. 16 is a schematic view of a state in which the shaft is inserted through the tube main body of the tube unit of the suction / liquid feeding unit of the treatment system according to the sixth embodiment, as viewed from the position along line 6A-6A in FIG.

  Hereinafter, embodiments for carrying out the present invention will be described with reference to the drawings.

(First embodiment)
The first embodiment will be described with reference to FIGS.
As shown in FIG. 1, the treatment system 10 according to this embodiment outputs appropriate power and / or signals in accordance with the operation of a treatment instrument (surgical device) 12 and switches 48a, 48b, and 48c described later. Energy source (controller) 14, suction / liquid feeding unit (suction / liquid feeding auxiliary tool) 16, fluid source 18, and suction device 20. The suction device 20 includes a suction source (suction pump) 20a and a suction tank 20b. The treatment instrument 12 is connected to an energy source 14 and used as an energy treatment instrument.

  The suction / liquid feeding unit 16 is used by being attached to the treatment instrument 12. A state where the suction / liquid feeding unit 16 is attached to the treatment instrument 12 is referred to as a treatment instrument unit 100. The suction / liquid feeding unit 16 is connected to the fluid source 18 and the suction device 20 for use. Here, although the example which uses the fluid source 18 as a liquid supply source is demonstrated, it is also possible to use it as an air supply source.

  The energy source 14 is connected to an input unit (not shown) for performing various settings.

  In this embodiment, the treatment instrument 12 includes a handle 32, a shaft 34, and an end effector 36. The handle 32, the shaft 34, and the end effector 36 define a longitudinal axis L of the treatment instrument 12. Since the longitudinal axis L is defined along the shaft 34 and / or the end effector 36, it may be straight or curved.

  The shaft 34 is supported by the handle 32 and protrudes along the longitudinal axis L toward the distal end side of the handle 32. The end effector 36 is disposed on the distal end side with respect to the distal end of the shaft 34 along the longitudinal axis L.

  The handle 32 is allowed to have various shapes. Here, a pistol type (gun type) will be described as an example. The handle 32 includes a housing 42 having a fixed handle (grip) 42a, and a movable handle 44 provided on the housing 42 and movable between a position separated from the fixed handle 42a and a position close thereto. The handle 32 has a rotation knob 46 at the distal end of the housing 42 for rotating the shaft 34 and the end effector 36 about the longitudinal axis L thereof. Since the relationship between the rotary knob 46, the shaft 34, and the end effector 36 is known, the description thereof is omitted here. The rotary knob 46 has a concave fixing portion (concave portion) 46a that receives a fixing arm 254 of a connecting portion 204 of a tube unit (liquid supply path) 94 described later. When the fixed arm 254 of the connecting portion 204 of the tube unit 94 is engaged with the fixed portion 46a, the tube unit 94 is rotated together with the shaft 34 and the end effector 36 according to the operation of the rotary knob 46.

  The handle 32 has switches 48 a and 48 b in the housing 42. For example, when the first switch 48 a is pressed, a signal is output from the energy source 14 to the fluid source 18, and a liquid such as physiological saline is supplied from the fluid source 18 to the tube unit 94 described later, and from the energy source 14 to be described later. Electric power, that is, energy (high-frequency energy) is supplied between the electrodes 72 and 82 to be operated. For example, when any of the second switch 48b, the third switch 48c, and a foot switch (not shown) is pressed, a signal is output from the energy source 14 to the suction source 20a. At this time, the suction source 20a is activated, suction is performed on the distal end side of the tube main body 212 through the tube main body 212 of the tube unit 94, and the suctioned material is stored in the suction tank 20b. When the pressed switch of the second switch 48b, the third switch 48c, and the foot switch (not shown) is released, a signal is output to the suction source 20a, and the operation of the suction source 20a is stopped.

  In the above description, the example in which the liquid supply is performed by electrically controlling the fluid source 18 has been described. When supplying the liquid from the fluid source 18, a method in which the energy source (controller) 14 does not perform control may be employed. In this case, the energy source 14 and the fluid source 18 do not need to be connected.

  For example, a liquid pack (fluid source 18) in which a liquid such as physiological saline is stored is suspended from a suspension base, and the liquid pack and the tube body 212 are connected by a tube, a connector, or the like. Then, using the atmospheric pressure and gravity applied to the liquid pack, physiological saline is dropped as in the drip.

  In the above description, the liquid suction by the suction source 20a is electrically ON / OFF controlled. A method in which the suction ON / OFF control is not performed by the suction source 20a may be adopted. For example, the suction by the suction source 20a may be continued while dripping the physiological saline from the liquid pack, or the suction by the suction source 20a is not performed during the treatment, and the liquid is sucked after the treatment is completed. Also good.

  As shown in FIG. 2A, the shaft 34 has a rod 52 whose tip is used as a second gripping portion 64 described later of the end effector 36, and a pipe 54 that covers the outer peripheral surface of the rod 52. The tip of the rod 52 protrudes toward the tip side along the longitudinal axis L with respect to the tip of the pipe 54. That is, the pipe 54 covers the outer peripheral surface of the rod 52 leaving the tip of the rod 52. The base end of the rod 52 is supported in the handle 32.

  As shown in FIG. 1, the end effector 36 has a pair of grip portions 62 and 64. Here, the first gripping portion 62 which is one of the pair of gripping portions 62 and 64 is formed to be movable. Although the description is omitted because it is publicly known, the movable first gripping portion 62 has a link mechanism 66 (FIG. 2A) interlocked with the operation of the movable handle 44 at a position where the movable handle 44 of the handle 32 is separated from the fixed handle 42a. (See FIG. 1) and is in the open position apart from the other second gripping portion 64 (see FIG. 1). When the movable handle 44 of the handle 32 is close to the fixed handle 42a, the movable first grip 62 is close to the other second grip 64 by the link mechanism 66 (see FIG. 2A). ).

  As shown in FIG. 2A, here, the end effector 36 of the treatment instrument 12 has a pair of electrodes 72 and 82, and performs treatment (for example, sealing of biological tissue) on a treatment target using bipolar high-frequency energy. An example will be described. In this embodiment, in order to perform treatment (for example, sealing of living tissue) using bipolar high-frequency energy, the first grasping portion 62 has the first electrode 72 and the second grasping portion 64 has the second electrode. An electrode 82 is provided. Of the tip of the rod 52, at least the position facing the first electrode 72 has conductivity. The second electrode 82 has a gripping surface (electrode surface) 82 a that grips the biological tissue to be treated in cooperation with the gripping surface 62 a of the first electrode 72. The gripping surface 82a can be visually recognized by the user.

  As shown in FIG. 2A, the first gripping portion 62 includes a first electrode 72 facing the second electrode 82 of the second gripping portion 64, and a side of the first electrode 72 that is separated from the second electrode 82. And a movable member 74 for covering. The first electrode 72 and the movable member 74 are formed such that the direction along the longitudinal axis L is longer than the width direction orthogonal to the longitudinal axis L. Here, the movable member 74 has a recess 74a for fixing the first electrode 72, an edge 74b (see FIG. 3B) formed outside the recess 74a, and the first electrode 72 fixed to the edge 74b. And a back surface 74c opposite to the other side (recess 74a). Usually, the recessed part 74a of the movable member 74 is not visually recognized by the user.

  As shown in FIGS. 2A and 3B, the first electrode 72 has an electrode surface 72a that contacts the living tissue to be treated. The edge 74b of the movable member 74 and the electrode surface 72a of the first electrode 72 cooperate to form a grasping surface 62a for grasping the living tissue to be treated. The gripping surface 62a can be visually recognized by the user.

  The back surface 74c of the movable member 74 shown in FIG. 2A is preferably formed in a smooth curved surface that can be prevented from being caught by a living tissue. The back surface 74c of the movable member 74 is formed in a curved surface shape such that the height with respect to the gripping surface 62a becomes smaller and the width becomes narrower toward the tip indicated by reference numeral 76a. Normally, the back surface 74c of the movable member 74 forms a part of the outer surface of the first grip portion 62, and is easily visually recognized by the user and easily touched by the user.

  In addition, when the 1st holding part 62 exists in a closed position with respect to the 2nd holding part 64, the 1st electrode 72 adjoins to a 2nd electrode. The first electrode 72 and the second electrode 82 are configured such that the first gripping portion 62 is in a closed position with respect to the second gripping portion 64 and is separated from each other even when the first electrode 72 is close to the second electrode. It is preferred that

  The aspirating / liquid feeding unit 16 shown in FIG. 1 cooperates with the first gripping portion 62 of the end effector 36 of the treatment instrument 12 to supply the liquid for the treatment instrument 12 that defines the flow path F to the biological tissue to be treated. And a tube unit 94 for supplying a liquid to the liquid delivery device 92. That is, the liquid delivery tool 92 is attached to the first gripping part 62 of the treatment tool 12 capable of grasping a living tissue and used as the treatment tool unit 100.

  If only the liquid feeding tool 92 is fed, a small diameter flexible tube may be used as the tube unit 94. In this embodiment, the tube unit 94 will be described as having a plurality of lumens (channels) capable of feeding and sucking liquid. The tube unit 94 according to this embodiment is used by being attached to the shaft 34 of the treatment instrument 12 and the rotation knob 46 of the handle 32. The liquid delivery tool 92 and the tube unit 94 are used in combination. The liquid delivery tool 92 and the tube unit 94 may be integrated when attached to the treatment tool 12, or may be separated from each other.

  As described above, the liquid delivery tool 92 shown in FIGS. 1 to 4 is mounted on the treatment instrument 12 and used as the treatment instrument unit 100. As shown in FIGS. 2A and 2B, the liquid delivery device 92 includes a main body (attachment body) 102 that can be attached to the first gripping portion 62 and a support portion 104 that is supported while being attached to the distal end portion of the shaft 34. And have. The main body 102 can rotate with respect to the support portion 104 via a pin 106. That is, the support portion 104 is attached to the treatment instrument 12 and pivotally supports a cover 112 described later so that the cover 112 can be rotated according to the rotation of the first grip portion 62. It should be noted that the rotation center of the first gripping portion 62 with respect to the shaft 34 of the end effector 36 of the treatment instrument 12 and the pin 106 that is the rotation center of the support portion 104 with respect to the main body 102 of the liquid delivery device 92 coincide with each other. preferable.

  As shown in FIGS. 2A to 4, the main body 102 includes a cup-shaped cover 112 that covers the distal end portion 76 of the back surface 74 c of the movable member 74 of the first gripping portion 62, and a port (channel) 114 that receives fluid from the outside. Have The cover 112 is continuous with the port 114 and defines a flow path F of a fluid such as a liquid supplied from the outside of the liquid delivery device 92. The cover 112 cooperates with the first grip portion 62 to form a flow path F continuous from the port 114, and grips the liquid received from the port 114 with an edge portion 112b, which will be described later, adjacent to the grip surface 62a of the cover 112. It flows out from between the edge part 74b of the surface 62a.

  The main body 102 has a pair of connecting portions 116 connected to the support portion 104 via a pair of pins 106. The connecting part 116 is formed on the base end side along the longitudinal axis L from the cover 112. The connecting portion 116 is located adjacent to the base end of the port 114. The pair of connecting portions 116 are separated from each other. The connecting portion 116 is provided with a holding arm (holding portion) 118 that holds the first gripping portion 62 so as to hold the vicinity of the proximal end portion of the movable member 74. The holding arm 118 is elastically deformable and urges the back surface 74c of the first gripping portion 62 and an edge portion 114a of the port 114 described later to be in close contact with each other.

  As shown in FIGS. 3A, 3B, and 4, when the liquid delivery device 92 is attached to the treatment device 12, the holding arm 118 holds the vicinity of the proximal end portion of the movable member 74, so that the main body 102 is It is attached to a movable member 74 of one gripping part 62. Therefore, the main body 102 rotates with respect to the support portion 104 via the pin 106 as the first gripping portion 62 moves to the open position (see FIG. 1). Similarly, as the first gripping part 62 moves to the closed position (see FIG. 3A), the main body 102 rotates with respect to the support part 104 via the pin 106. That is, the holding unit 118 holds the state where the cover 112 and the port 114 rotate together with the first gripping unit 62. The pin 106 may be formed integrally with the main body 102 or may be formed integrally with the support portion 104.

  2A and 2B, it is preferable that the cover 112, the port 114, the pair of connecting portions 116, and the pair of holding arms 118 are integrally formed.

  As shown in FIGS. 2A, 2B, and 3A to 4, the cover 112 covers an inner periphery that covers the vicinity of the distal end portion 76 including the distal end 76a of the back surface 74c of the movable member 74 of the first grasping portion 62 of the treatment instrument 12. A surface 112a is provided. As shown in FIGS. 2A and 2B, the cover 112 is formed in a substantially ¼ spherical shape. As shown in FIG. 2B, the cover 112 has a substantially U-shaped edge 112 b at a position facing the second grip portion 64.

  As shown in FIG. 3A and FIG. 3B, the position of the edge portion 112 b facing the front end 76 a of the back surface 74 c of the movable member 74 of the first gripping portion 62 indicated by reference numeral 112 c is the movable member of the first gripping portion 62. 74 is separated from the tip 76a of the back surface 74c of 74. For this reason, a gap G is formed between the inner peripheral surface 112 a of the cover 112 and the front end portion 76 of the back surface 74 c of the movable member 74 of the first gripping portion 62.

  As shown in FIGS. 2A to 2C, in this embodiment, the port 114 is formed in a half-pipe shape such as a substantially U-shaped cross section orthogonal to the longitudinal axis L. As shown in FIGS. 3A and 4, the port 114 is fitted with a first conduit 214, which will be described later, as a liquid feeding pipe of the tube unit 94. For example, it is preferable that the width of the port 114 is gradually reduced from the proximal end side toward the distal end side. For this reason, it is easy to maintain the fitting state of the first conduit 214 described later of the tube unit 94 to the port 114.

  As shown in FIGS. 1, 3A, and 4, a first conduit (liquid feeding tube) 214, which will be described later, of the tube unit 94 is disposed between the pair of connecting portions 116.

  As shown in FIGS. 3A and 3C, the port 114 forms a fluid flow path F by a gap G between the port 114 and the back surface 74 c of the movable member 74. It is preferable that the proximal end portion of the edge 114 a of the port 114 and the back surface 74 c of the movable member 74 are in close contact with each other. It is also preferable that a sealing material such as a rubber material is fixed to the edge portion 114a of the port 114 shown in FIGS. 2A to 2C.

  As shown in FIG. 3A, the base end of the port 114 is maintained in close contact with the back surface 74c of the movable member 74 in a state where the liquid feeding device 92 is attached to the first gripping portion 62, and the distal end of the port 114 is movable. The member 74 is kept away from the back surface 74c. For this reason, the tip of the port 114 communicates with the gap G between the cover 112 and the back surface 74 c of the movable member 74 of the first gripping part 62.

  The liquid delivery tool 92 forms a gap G with respect to the distal end portion 76 of the back surface 74 c of the movable member 74 of the first gripping portion 62 from the distal end of the port 114 to the distal end 112 c of the edge portion 112 b of the cover 112. . Therefore, the flow path F is defined from the tip of the port 114 to the tip 112c of the edge 112b of the cover 112.

  As shown in FIGS. 1 to 4, the support portion 104 may have a cylindrical portion 132 fitted to the outer peripheral surface 35 of the shaft 34. A part of the cylindrical portion 132 forms a guide portion 134 that allows the movement of the first conduit 214 of the tube unit 94 and guides the movement. When the first grip portion 62 and the main body 102 of the liquid feeding device 92 are rotated by the guide portion 134, the gap between the first conduit 214 of the tube 202 of the tube unit 94 and the port 114 of the main body 102 of the liquid feeding device 92 is rotated. Is prevented from being loaded. Therefore, the fitting between the first conduit 214 of the tube unit 94 and the main body 102 of the liquid delivery device 92 is maintained. Further, the state in which the main body 102 of the liquid delivery tool 92 is fitted to the first grip portion 62 is maintained.

  In addition, it is ensured that the liquid delivery device 92 is not detached from the first gripping portion 62 of the treatment instrument 12 during the treatment of the living tissue with the main body 102 of the liquid delivery device 92 attached to the first gripping portion 62. If it is, the support part 104 is not necessarily required. In the present embodiment, even if the main body 102 of the liquid delivery device 92 is unintentionally detached from the first gripping portion 62, the state in which the support portion 104 is attached to the treatment instrument 12 (shaft 34) is maintained. It is ensured that the liquid delivery device 92 (main body 102) does not come off the treatment device 12.

  As shown in FIG. 1, the tube unit 94 includes a tube 202 that is used by being attached to the outside of the pipe 54 of the shaft 34, and a connecting portion 204 that is fixed to the proximal end of the tube 202 and connected to the rotary knob 46. Have. The tube 202 is made of a flexible material such as a silicone material, a polyurethane material, or a polyethylene material.

  As shown in FIG. 5, the tube 202 includes a cylindrical main body (outer tube) 212 and a first conduit (front end side conduit) 214 protruding from the front end 212 a of the main body 212 to the front end side. The main body 212 extends along a central axis (longitudinal axis) C defined by the distal end 212a and the proximal end 212b (see FIG. 8A). The main body 212 and the first conduit 214 are preferably formed integrally. As shown in FIGS. 5, 6 </ b> A, and 6 </ b> B, the main body 212 includes a plurality of (here, four) protrusions (ribs) 222, 224, 226, and 228 that protrude radially inward. The protrusions 222, 224, 226, 228 are provided along the central axis C.

  The protrusions 222, 224, 226, and 228 have protrusion surfaces 222a, 224a, 226a, and 228a, and a pair of side surfaces 222b, 224b, 226b, and 228b, respectively. The projecting surfaces 222 a, 224 a, 226 a, and 228 a are at positions projecting inward in the radial direction of the tube main body 212 with respect to the inner peripheral surface 213 a of the tube main body 212. The protruding surfaces 222 a, 224 a, 226 a, 228 a are in contact with the outer peripheral surface 35 of the shaft 34. A pair of side surfaces 222b, 224b, 226b, 228b is formed between the projecting surfaces 222a, 224a, 226a, 228a and the inner peripheral surface 213a of the tube body 212, respectively. The pair of side surfaces 222b, 224b, 226b, and 228b have normals directed in substantially opposite directions.

  The main body 212 and the plurality of protrusions 222, 224, 226, 228 are preferably formed integrally. The protrusions 222, 224, 226, and 228 are preferably formed at appropriate intervals in the circumferential direction with respect to the central axis C of the main body 212. Here, the protrusions 222, 224, 226, and 228 are formed at intervals of 90 ° in the circumferential direction with respect to the central axis C of the main body 212. The protrusions 222, 224, 226, and 228 are preferably formed continuously from the distal end 212a (see FIG. 5) to the proximal end 212b (see FIG. 8A) of the main body 212 of the tube 202. The tip 212a of the main body 212 of the tube 202 is used as a suction opening. The base end 212 b of the main body 212 of the tube 202 is used as a suction guide portion that communicates with the second port 258 in the connecting portion 204.

  As shown in FIGS. 5 to 6B, a flow path (liquid feeding conduit) 232 is formed in one of the plurality of protrusions 222, 224, 226, and 228. The flow path 232 of the protrusion 222 can pass the liquid that flows in from the proximal end 212b (see FIG. 8A) of the tube main body 212 and flows out from the distal end 212a. The flow path 232 communicates with the flow path 214a of the first conduit 214 protruding from the distal end of the tube 202 toward the distal end side.

  As shown in FIG. 8A, in this embodiment, the tube 202 has a second conduit (base-end-side conduit) 216 serving as a liquid feeding tube protruding from the base end 212b of the main body 212 to the base end side. The main body 212 and the second conduit 216 are preferably formed integrally. The flow path 232 communicates with the flow path 216 a of the second conduit 216. Therefore, a fluid such as a liquid can flow from the channel 216 a of the second conduit 216 to the channel 214 a of the first conduit 214 through the channel 232 of the main body 212. Therefore, a fluid such as a liquid can flow out from the tip of the flow path 214a of the first conduit 214.

  As shown in FIG. 6B, with the shaft 34 of the treatment instrument 12 disposed inside the tube 202, between the protrusions 222 and 224, between the protrusions 224 and 226, between the protrusions 226 and 228, and Lumens 223, 225, 227, and 229 are formed between the protrusions 228 and 222, respectively. That is, the main body 212 of the tube unit 94 forms a plurality of lumens 223, 225, 227, and 229 in cooperation with the shaft 34 of the treatment instrument 12.

  The protrusion 222 cooperates with the inner peripheral surface 213a of the tube main body 212 and the outer peripheral surface 35 of the shaft 34 to form lumens 223 and 229 at positions adjacent to each other in the circumferential direction. The protrusion 224 forms lumens 223 and 225 at positions adjacent to each other in the circumferential direction. The protrusion 226 forms lumens 225 and 227 at positions adjacent to each other in the circumferential direction. The protrusion 228 forms lumens 227 and 229 at positions adjacent to each other in the circumferential direction.

  As shown in FIG. 5, the tube body 212 has through holes 223a and 229a penetrating the inner peripheral surface 213a and the outer peripheral surface 213b in the vicinity of the tip 212a. When clogging occurs at the ends of the lumens 223 and 229 shown in FIG. 5, suction is performed from the through holes 223 a and 229 a formed on the side surface of the main body 212. Needless to say, the lumens 225 and 227 are also preferably formed with through holes (not shown).

  As shown in FIGS. 7A to 8B, the connecting portion 204 includes a cylindrical main body (housing) 252, a fixed arm (fixed portion) 254, a first port (liquid feeding port) 256, and a second port (suction). Port) 258. The main body 252 has a first through-hole 252a into which the tube main body 212 is inserted at the tip thereof, and a second through-hole 252b into which the shaft 34 is inserted at the other end. An O-ring 260a is provided as a first seal member at the edge of the first through hole 252a, and an O-ring 260b is provided as a second seal member at the edge of the second through hole 252b. The O-ring 260 a on the distal end side is in close contact with the outer peripheral surface 213 b of the main body 212 of the tube 202. That is, the first seal member 260 a seals between the outer peripheral surface 213 b of the tube main body 212 and the main body 252 of the connecting portion 204. The proximal-side O-ring 260 b is in close contact with the outer peripheral surface 35 of the shaft 34 of the treatment instrument 12. That is, the second seal member 260 b seals between the outer peripheral surface 35 of the shaft 34 and the main body 252 of the connecting portion 204.

  The first port 256 is provided in the main body 252 of the connecting portion 204 and communicates with the second conduit 216 of the tube 202. The first port 256 is used for liquid feeding in this embodiment. The first port 256 is connected to the fluid source 18 shown in FIG. 1 through the tube 22a. Note that the first port 256 may be used for air supply.

  The second port 258 is provided in the main body 252 of the connecting portion 204 and communicates the inside and the outside of the main body 252. The base end 212 b of the main body 212 of the tube 202 and the second port 258 communicate with each other inside the main body 252 of the connecting portion 204. That is, the second port 258 communicates with the proximal end 212 b of the tube body 212. The second port 258 is used for suction in this embodiment. The second port 258 is connected to the suction tank 20b shown in FIG. 1 through the tube 22b.

  As shown in FIGS. 7A and 7B, the fixed arm 254 is fixed to the concave fixing portion 46 a of the rotary knob 46. For example, when there is one fixed arm 254 and one fixed portion 46a corresponding to the fixed arm 254, the direction of the suction / liquid feeding unit 16 is determined. At this time, the fixed arm 254 is fixed to the rotary knob 46 in both the direction along the longitudinal axis L and the direction around the longitudinal axis L. Therefore, when the rotary knob 46 is rotated around the longitudinal axis L in a state where the fixed arm 254 is fixed to the rotary knob 46, the tube 202 outside the shaft 34 also rotates together.

  As shown in FIG. 1, the treatment instrument 12, the energy source 14, the fluid source 18 and the suction source 20a can transmit and receive electrical signals. Therefore, when the switch 48a is pressed, a signal is transmitted from the energy source 14 to the fluid source 18, the fluid source 18 is driven, and high-frequency energy is output from the energy source 14. Further, when the switch 48b is pressed, a signal is transmitted from the energy source 14 to the suction source 20a, and the suction source 20a is driven.

  The flow rate of the fluid supplied from the fluid source 18 when the switch 48a of the treatment instrument 12 is pressed, the lengths of the channels 216a, 232, 214a of the tube unit 94, the cross-sectional areas of the channels 216a, 232, 214a, etc. An appropriate time is input to the energy source 14, and the time from when the switch 48a is pressed until the high-frequency current is output from the energy source 14 is calculated. For this reason, the timing at which the liquid flows out to the gripping surface 62a of the first gripping portion 62 of the end effector 36 and the output timing of the high-frequency current can be adjusted. In addition, a high-frequency current may be output after the sensor or the like recognizes that the liquid has passed through an appropriate position of the tube unit 94.

  When supplying the liquid with the fluid source 18 of the liquid pack that does not electrically control the supply of the liquid, the liquid pack storing the liquid such as physiological saline is suspended from the suspension base. A saline solution is dropped like an infusion using the atmospheric pressure and gravity applied to the liquid pack by connecting the liquid pack and the tube main body 212 with a tube or a connector. Although not shown, an adjustment device that adjusts the flow rate of liquid flowing in the tube by pressing the tube and deforming the tube is attached to the tube, and the flow rate of the dropped liquid is adjusted by the operator. Can be adjusted as appropriate.

  Next, the operation of the treatment system 10 according to this embodiment will be described. Here, an example in which physiological saline is used as the liquid supplied from the fluid source 18 will be described. Here, an example will be described in which coagulation / sealing of a living tissue to be treated is performed using high-frequency current (high-frequency energy) as energy for treating the living tissue. A blood vessel will be described as an example of a biological tissue to be treated.

  The suction / liquid feeding unit (auxiliary tool) 16 shown in FIG. 1 is created by fitting the first conduit 214 of the tube unit 94 from the base end side of the port 114 of the main body 102 of the liquid feeding tool 92 shown in FIG. 2A. To do. At this time, the first conduit 214 of the tube unit 94 passes inside the support portion 104 of the liquid delivery device 92. The suction / liquid feeding unit 16 may be created by fixing the first conduit 214 of the tube unit 94 to the main body 102 of the liquid feeding tool 92 by adhesion or welding.

  As shown in FIG. 1, the end effector 36 of the treatment instrument 12 is opposed to the proximal through hole 252 b of the connecting portion 204 of the tube unit 94. The movable handle 44 of the handle 32 is moved close to the fixed handle 42 a to move the first gripping portion 62 to the closed position with respect to the second gripping portion 64. In this state, the end effector 36 of the treatment instrument 12 is projected to the distal end side of the distal end 212 a of the tube main body 212 through the connecting portion 204 of the tube unit 94 and the tube main body 212. At this time, the longitudinal axis L of the treatment instrument 12 and the central axis (longitudinal axis) C of the tube unit 94 coincide with each other. Then, as shown in FIGS. 3A to 4, the inner peripheral surface 112 a of the cover 112 of the liquid feeding device 92 is opposed to the distal end portion 76 of the back surface 74 c of the movable member 74 of the first gripping portion 62 of the end effector 36. Let At this time, the holding arm 118 of the main body 102 of the liquid delivery device 92 holds the vicinity of the proximal end portion of the movable member 74 of the first gripping portion 62 by snap fitting. For this reason, the main body 102 of the liquid delivery tool 92 is attached to the movable member 74 of the first grip portion 62.

  When the inner peripheral surface 112a of the cover 112 of the liquid feeding device 92 is opposed to the back surface 74c of the movable member 74 of the first gripping portion 62 of the end effector 36, the first conduit 214 of the tube unit 94 is connected to the liquid feeding device 92. It is fixed to the back surface 74 c of the movable member 74 of the first gripping part 62 in a state of being disposed in the port 114. At this time, the tip of the port 114 and the tip of the first conduit 214 are spaced apart. A gap G, that is, a flow path F is formed between the vicinity of the front end of the port 114 and the back surface 74 c of the movable member 74.

  The operator appropriately operates the movable handle 44 and confirms the follow-up operation of the main body 102 of the liquid delivery device 92 with respect to the movable member 74 of the first gripping portion 62.

  In the tube unit 94, the proximal end of the main body 252 of the connecting portion 204 abuts or approaches the distal end of the rotation knob 46. In this state, as shown in FIGS. 7A and 7B, the fixed arm 254 of the connecting portion 204 is fitted into the fixed portion 46 a of the rotary knob 46, and the fixed arm 254 is fixed to the rotary knob 46. For this reason, when the rotation knob 46 is rotated, the connecting portion 204 of the tube unit 94 rotates following the rotation of the rotation knob 46.

  The surgeon places the end effector 36 in the body cavity with the suction / liquid feeding unit 16 attached to the treatment instrument 12. The position and posture of the end effector 36 are confirmed using, for example, an endoscope (not shown).

  The surgeon appropriately operates the movable handle 44 and grips the blood vessel using the distal end portion (distal region) of the gripping surface 62 a of the first gripping portion 62. When the operator presses the first switch 48a, the fluid is supplied from the fluid source 18 to the main body 102 of the liquid delivery device 92 through the tube 22a, the first port 256, and the tube 202, and from the energy source 14 to the gripping portion. High-frequency electrical energy is supplied between the electrodes 72 and 82 of the 62 and 64.

  The liquid is discharged from the tip of the first conduit 214 toward the tip of the port 114 of the liquid delivery device 92. The distal end of the port 114 communicates with a gap G between the inner peripheral surface 112 a of the cover 112 and the distal end portion 76 of the back surface 74 c of the movable member 74 of the first gripping portion 62.

  Here, the liquid delivery tool 92 is spaced from the front end of the port 114 to the front end 112c of the edge 112b of the cover 112 with respect to the front end 76 of the back surface 74c of the movable member 74 of the first gripping part 62, that is, A flow path F is formed. For this reason, the fluid flows through the flow path F (gap G). In particular, the back surface 74c of the movable member 74 has a height that is smaller with respect to the gripping surface 62a toward the front end indicated by reference numeral 76a, so that the liquid flows toward the front end 76a of the front end portion 76 of the rear surface 74c of the movable member 74. easy. The liquid passes between the front end portion 76 of the back surface 74c of the movable member 74 of the first gripping portion 62 and the inner peripheral surface 112a of the cover 112 of the liquid delivery device 92, and the back surface 74c of the movable member 74 of the first gripping portion 62. From between the tip 76a of the cover and the edge 112b of the cover 112, the paper is discharged to the gripping surface 62a. In this embodiment, physiological saline is allowed to flow from the tip of the gripping surface 62a of the first gripping part 62 to the blood vessel to be treated. In other words, in the suction / liquid feeding unit 16 and the treatment instrument unit 100 according to this embodiment, the position where the physiological saline flows through the blood vessel is set to the tip of the grip surface 62 a of the first grip portion 62. As described above, the flow path F between the cover 112 and the back surface 74c of the movable member 74 of the first gripping portion 62 of the treatment instrument 12 is the tip of the edge portion 112b adjacent to the gripping surface 62a of the cover 112. 112c and the edge 74b of the holding surface 62a. For this reason, the liquid flows out from between the front end 112c of the cover 112 and the edge 74b of the gripping surface 62a.

  As described above, the treatment system 10 according to this embodiment treats a treatment target of a living tissue using high-frequency energy while applying a liquid such as physiological saline to the treatment target of the living tissue. The physiological saline is allowed to flow only to the tip of the grasping surface 62a of the first grasping part 62 that grasps the biological tissue to be treated. For this reason, energy is efficiently supplied to the site | part to which the physiological saline was apply | coated among the biological tissues of treatment object.

  The grasped blood vessel is sealed after the protein is denatured by the action of physiological saline and high-frequency energy. At this time, the grasped blood vessel is prevented from sticking to the grasping surface 62a by the action of physiological saline. For this reason, for example, when the movable handle 44 is released and the first gripping portion 62 is moved to the open position with respect to the second gripping portion 64, the sealed state of the blood vessel is maintained. Further, when high frequency energy is applied to the blood vessel, the grasped blood vessel is prevented from being carbonized by the action of physiological saline.

  By the way, when physiological saline is flowed over the entire gripping surface 62a of the first gripping portion 62, energy is also used for a portion that is not gripping the living tissue. As in this embodiment, by flowing physiological saline from the distal end of the gripping surface 62a (the distal end of the movable member 74) 76a of the first gripping portion 62 to the biological tissue to be treated, energy can be efficiently passed. Can be added to the organization. For this reason, even if the same energy is used, the physiological saline is applied only to the tip 76a of the gripping surface 62a of the first gripping part 62, rather than the physiological saline is applied to the entire gripping surface 62a of the first gripping part 62. When applied, energy can be used more efficiently. Therefore, even if the same energy is used, the physiological saline is applied only to the tip 76a of the gripping surface 62a of the first gripping portion 62, rather than the physiological saline is applied to the entire gripping surface 62a of the first gripping portion 62. By doing so, blood vessel hemostasis can be performed early and reliably.

  Here, an example in which the gap G is formed at the tip 112c of the edge 112b with respect to the tip 76 of the back surface 74c of the movable member 74 of the first gripping portion 62 has been described. The position indicated by reference numeral 112c, that is, the opening of the gap G may be formed at any position of the edge 112b. That is, the position indicated by reference numeral 112 c is preferably at the tip of the cover 112, but may be formed at any edge 112 b of the cover 112. Further, when hemostasis is performed in other biological tissues such as hepatocytes, the distal end portion (the region on the distal end side) of the grasping surface 62a of the first grasping portion 62 is used as a treatment target, as in the case of sealing a blood vessel. Grasping the living tissue. The liver has a high blood vessel density, and thin blood vessels are distributed at a high density. When a thin blood vessel that appears in the middle of applying a treatment to a liver cell is difficult to grasp by the first grasping portion 62 and the second grasping portion 64, first, the first grasping portion 62 is opened with respect to the second grasping portion 64. The treatment target is brought into contact with the living tissue so that the treatment target is positioned between 62 and the second grasping portion 64. Next, physiological saline is flowed from the tip of the gripping surface 62a of the first gripping portion 62 (tip of the movable member 74) 76a to the living tissue to be treated, and between the first gripping portion 62 and the second gripping portion 64. Electrical connection is made through saline. And a high frequency current is output, a high frequency current can be sent through a physiological saline to a treatment object, and a blood vessel can be hemostatic.

  In this embodiment, four lumens 223, 225, 227, and 229 are formed between the outer peripheral surface 35 of the shaft 34 and the inner peripheral surface 213a of the main body 212 of the tube unit 94. When suction by the suction source 20a of the suction device 20 is applied to the second port 258 of the connecting portion 204, the pressure between the inner peripheral surface 213a of the tube main body 212 and the outer peripheral surface 35 of the shaft 34 is reduced. At this time, the outer peripheral surface 35 of the shaft 34 is formed of a hard material such as a stainless steel material. As described above, the tube body 212 is formed of a flexible soft material such as a silicone material, a polyurethane material, or a polyethylene material. For this reason, when a suction force is applied between the outer peripheral surface 35 of the shaft 34 and the inner peripheral surface 213a of the tube main body 212, the protrusions (ribs) 222 and 224 of the tube main body 212 and the protrusions 224 and 226 are included. The inner peripheral surface 213a between the protrusions 226 and 228 and between the protrusions 228 and 222 approaches or abuts the outer peripheral surface 35 of the shaft 34, respectively. As the inner peripheral surface 213a of the tube body 212 approaches or comes into contact with the outer peripheral surface 35 of the shaft 34, the projecting surfaces 222a, 224a, 226a, 228a of the protrusions 222, 224, 226, 228 become the outer peripheral surface of the shaft 34. 35. At this time, the protrusions 222, 224, 226, and 228 maintain their shapes. That is, the protrusions 222, 224, 226, and 228 are distances between the inner peripheral surface 213 a of the tube main body 212 and the protruding surfaces 222 a, 224 a, 226 a, and 228 a in a state where negative pressure is applied to the inside of the tube main body 212 ( That is, the inward protruding length) is maintained.

  For this reason, even if a part of the inner peripheral surface 213a of the tube main body 212 is in close contact with the outer peripheral surface 35 of the shaft 34 due to the suction force, the protrusions 222, 224, 226, and the like on the inner peripheral surface 213a of the tube main body 212. Spaces S are maintained at positions adjacent to the pair of side surfaces 222b, 224b, 226b, and 228b of 228, respectively. That is, when a negative pressure is applied to the inside of the tube main body 212, a space is formed between the pair of side surfaces 222b, 224b, 226b, 228b and the outer peripheral surface 35 of the shaft 34 by the inner peripheral surface 213a of the tube main body 212. S is formed. Therefore, the space S is maintained as a suction path, and physiological saline, blood, and biological tissue are guided by suction from the distal end 212a of the tube main body 212 toward the proximal end 212b, and the suction tank 20b is passed through the second port 258 and the tube 22b. To be discharged.

  At this time, a plurality of lumens 223, 225, 227, and 229 are formed between the inner peripheral surface 213 a of the tube main body 212 and the outer peripheral surface 35 of the shaft 34. For this reason, the tube main body 212 only needs to have the inner peripheral surface 213a to form the lumens 223, 225, 227, and 229, and can suppress an increase in thickness.

  For example, even if one lumen 223 is clogged, the remaining lumens 225, 227, and 229 ensure communication between the distal end 212a and the proximal end 212b. For this reason, the tube body 212 can secure a suction path.

  In the body cavity, for example, the separated biological tissue is taken out from the body cavity by using forceps, and physiological saline, blood, and the like are removed by suction. In addition, when physiological saline is used as described above, mist is generated, which may hinder viewing the end effector 36 with an endoscope. At this time, by performing suction by operating the second switch 48b, it is possible to eliminate the work of grasping the living tissue with forceps and taking it out from the body cavity. In addition, mist generated by treatment or the like can be quickly removed.

  As described above, according to the treatment system 10 according to this embodiment, the following can be said.

  By using the treatment instrument unit 100 in which the liquid delivery tool 92 is attached to the treatment instrument 12, the first gripping part is formed by the flow path F formed between the liquid delivery tool 92 and the first gripping part 62 of the treatment tool 12. Of 62, a liquid such as physiological saline can be dropped at a desired position. For this reason, a biological tissue can be treated using energy. For this reason, it is possible to perform the treatment by efficiently applying energy to the treatment target while causing the liquid to flow out and reducing the energy loss.

  Further, it is possible to perform suction using the tube unit 94 in cooperation with the treatment instrument 12. At this time, the tube unit 94 can form a plurality of lumens in cooperation with the treatment instrument 12. In particular, even if negative pressure is applied to the tube body 212 by the protrusions 222, 224, 226, and 228, the shape of the protrusions 222, 224, 226, and 228 is maintained. A space S can be formed at a position adjacent to 228. The space S can be used as a suction path. For this reason, in order to eliminate the clogging of the suction path, there is no need to secure the suction path by temporarily removing the treatment portion of the treatment tool from the body. Therefore, by using the tube unit 94 according to this embodiment, the sucked material can be efficiently stored in the suction tank 20b.

  In this embodiment, the end effector 36 of the type in which the first gripping portion 62 moves with respect to the second gripping portion 64 has been described as an example. That is, the example in which the first gripping part 62 is movable with respect to the second gripping part 64 fixed has been described. As shown in FIG. 10, it is also preferable to use an end effector 36 of a type in which both the first and second gripping portions 62 and 64 move. That is, it is also preferable that both the first gripping portion 62 and the second gripping portion 64 have a structure that can be relatively close to and separated from each other. In this case, the liquid delivery tool 92 may be used by being attached to either of the first and second gripping portions 62 and 64. Moreover, you may attach the liquid feeding tool 92 to both the 1st and 2nd holding | gripping parts 62 and 64. FIG.

  It is also preferable to arrange an appropriate device in a part of the lumens 223, 225, 227, 229 on the outer periphery of the shaft 34. That is, as shown in FIG. 10, the plurality of lumens 223, 225, 227, and 229 can be used as insertion paths for various treatment devices. Among the plurality of lumens 223, 225, 227, and 229, the liquid delivery catheter 304 is inserted into one lumen 223. A snare 302 is inserted through another lumen 225. These treatment devices (liquid feeding catheter 304 and snare 302) can be used together with the treatment instrument 12.

  The liquid delivery catheter 304 is disposed, for example, in the lumen 223 separately from the flow path 216a of the second conduit 216, the flow path 232 of the main body 212, and the flow path 214a of the first conduit 214. And the liquid delivery catheter 304 can apply | coat a chemical | medical solution etc. to a desired position, for example. The snare 302 is disposed in the lumen 225, for example. For example, the snare 302 can bind and cut off an object to be cut such as a polyp. Using the same lumen 225 or other lumens 223, 227, 229, the object to be excised can be aspirated and the object to be excised can be stored in the suction tank 20b.

  In addition, although the treatment tool 12 according to the first embodiment has been described with respect to an example using high-frequency energy, thermal energy generated by a heater may be used together with high-frequency energy or instead of high-frequency energy. For example, when heat energy is used together with high frequency energy, a heater may be disposed between the electrode 72 and the movable member 74. For example, a heater may be disposed on the back surface of the electrode 72. For example, when heat energy is used instead of high-frequency energy, the electrode 72 may be replaced with a heat transfer plate or a heater.

  Further, the example in which the second grip portion 64 uses high-frequency energy in cooperation with the first electrode 72 has been described. In addition, ultrasonic vibration may be transmitted to the rod 52 of the shaft 34. When the living tissue is grasped between the first and second grasping portions 62 and 64, high-frequency energy is used and ultrasonic vibration is transmitted to the rod 52, the living tissue can be cut while being sealed.

(Second Embodiment)
Next, a second embodiment will be described with reference to FIGS. 11A to 12C. This embodiment is a modification of the first embodiment including a modification, and the same members or members having the same functions as those described in the first embodiment are denoted by the same reference numerals as much as possible. Is omitted.

  As shown in FIG. 11A, in this embodiment, the port 114 of the main body 102 of the liquid delivery device 92 has a cylindrical pipe 114b instead of a half pipe. The outer peripheral surface of the pipe 114b is in contact with or in close contact with the back surface 74c of the movable member 74. The tip of the port 114 communicates with the gap G. The pipe 114b may be formed of a soft material having flexibility similar to that of the tube main body 212, or may be formed of a hard material such as a hard plastic material or a metal material.

  In the first embodiment, in order to fix the main body 102 of the liquid delivery device 92 to the first gripping portion 62 of the treatment instrument 12, a holding arm (holding portion) 118 is attached to the connecting portion 116 of the main body 102 of the liquid delivery device 92. An example in which is provided has been described. Here, an example will be described in which the cover 112 is provided with a fitting portion 112d that fits the edge 74b of the movable member 74 of the first gripping portion 62. In addition, it is also preferable that both the holding arm 118 and the fitting portion 112d are formed in the main body 102 of the liquid delivery tool 92.

  As shown in FIG. 12C, the fitting portion 112 d protrudes inward from the edge portion of the cover 112. The inner peripheral surface 112 a of the cover 112 supports a position of the distal end portion 76 of the movable member 74 that is close to the edge portion 74 b. The fitting portion 112d can hold the edge portion 74b of the movable member 74. For this reason, the fitting portion 112d is fitted to the edge portion 74b of the gripping surface 62a. In other words, the fitting portion 112 d maintains a state where the cover 112 and the port 114 rotate together with the first gripping portion 62.

  At this time, as shown in FIGS. 12A and 12B, a gap G (flow path F) similar to that described in the first embodiment is formed.

  In this state, when the switch 48 a is pressed, the fluid source 18 is activated, and the tube 22 a from the fluid source 18, the first port 256 of the tube unit 94, the cylindrical main body 252 of the connecting portion 204, and the second conduit of the tube unit 94. The channel between the port 114 of the liquid delivery device 92 and the back surface 74c of the first gripping part 62 through the channel 216a of 216, the channel 232 of the protrusion 222 of the tube body 212, and the channel 214a of the first conduit 214. A liquid is supplied to F. For this reason, the liquid is supplied to the outer periphery of the blood vessel from between the distal end of the movable member 74 of the first gripping portion 62 and the distal end of the liquid delivery tool 92. In this state, the energy source 14 applies a high-frequency current (high-frequency energy) between the first electrode 72 and the second electrode 82 to appropriately seal the blood vessel.

  At this time, when a liquid such as physiological saline is supplied to the blood vessel, the physiological saline is mainly flowed to the distal end side of the gripping surface 62a, and the physiological saline is difficult to flow to the proximal end side. For this reason, the blood vessel can be sealed using energy efficiently. By supplying physiological saline to the gripping surface 62 a, the blood vessel that has been once sealed and bonded is attached to the first gripping portion 62 when the first gripping portion 62 is opened with respect to the second gripping portion 64. Therefore, it is possible to suppress the release of the blood vessel seal.

(Third embodiment)
Next, a third embodiment will be described with reference to FIG. This embodiment is a modification of the first and second embodiments, and the same members or members having the same functions as those described in the first and second embodiments are given the same reference numerals as much as possible. Detailed description is omitted.

  In the first and second embodiments, the example in which the first electrode 72 is fixed to the movable member 74 has been described. Here, as shown in FIG. 13, the movable member 74 rotates the gripping surface 62a in a wiper shape or a seesaw shape in accordance with the living tissue. Specifically, a rotating body (electrode holding member) 78 is rotatably supported by the movable member 74 by a pin 78a. The rotating body 78 holds the electrode 72.

  Here, the back surface 74c of the movable member 74 is formed in the same manner as described in the second embodiment. For this reason, as described in the second embodiment, treatment can be appropriately performed while flowing the liquid. Of course, it is preferable to use the port 114 described in the first embodiment.

(Fourth embodiment)
Next, a fourth embodiment will be described with reference to FIGS. 14A and 14B. This embodiment is a modification of the first to third embodiments, and the same members or members having the same functions as those described in the first to third embodiments are given the same reference numerals as much as possible. Detailed description is omitted.

  Here, a modified example of the tube 202 of the tube unit 94 will be described.

  As shown in FIG. 14A, the protrusions 222, 224, and 226 are formed every 60 ° with respect to the central axis C. As shown in FIG. 14B, the protrusion 222 forms lumens 223 and 227 with the shaft 34 inserted through the tube 202. The protrusion 224 forms lumens 223 and 225. The protrusion 226 forms lumens 225 and 227. In this state, when a negative pressure is applied to the tube 202, the inner peripheral surface 213a of the tube main body 212 can be in contact with or in close contact with the outer periphery of the shaft 34, as indicated by a broken line in FIG. 14B. Even in this case, the protrusions 222, 224, and 226 are distances between the inner peripheral surface 213a of the tube body 212 and the protruding surfaces 222a, 224a, and 226a in a state where negative pressure is applied to the inside of the tube body 212. (Ie, the inward protruding length) is maintained. Spaces S are respectively formed at positions adjacent to the protrusion 222 in the circumferential direction, positions adjacent to the protrusion 224 in the circumferential direction, and positions adjacent to the protrusion 226 in the circumferential direction. For this reason, the space S is maintained as a suction path.

(Fifth embodiment)
Next, a fifth embodiment will be described with reference to FIGS. 15A and 15B. This embodiment is a modification of the first to fourth embodiments, and the same members or members having the same functions as those described in the first to fourth embodiments are denoted by the same reference numerals as much as possible. Detailed description is omitted.

  Here, a modified example of the tube 202 of the tube unit 94 will be described.

  As shown in FIG. 15A, only one protrusion 222 is formed on the inner peripheral surface 213 a of the main body 212 of the tube 202 of the tube unit 94. As shown in FIG. 15B, when the shaft 34 is inserted into the tube 202, the outer periphery of the shaft 34 comes into contact with the protruding surface 222a of the protruding portion 222, and the protruding surface 222a of the inner peripheral surface 213a of the tube main body 212 is contacted. The opposing position contacts the outer periphery of the shaft 34. In this state, the protrusion 222 forms lumens 223 and 225. At this time, unlike the first and fourth embodiments, the central axis C of the tube 202 and the longitudinal axis L of the shaft 34 do not coincide with each other and are in a shifted position.

  In this state, when a negative pressure is applied to the tube 202, the inner peripheral surface 213a of the tube main body 212 comes into close contact with the outer periphery of the shaft 34, as indicated by a broken line in FIG. The protrusion 222 maintains the distance between the inner peripheral surface 213a of the tube body 212 and the protrusion surface 222a in a state where negative pressure is applied to the inside of the tube body 212. Even in this case, a space S is formed at a position adjacent to the protrusion 222 in the circumferential direction. For this reason, the space S is maintained as a suction path.

(Sixth embodiment)
Next, a sixth embodiment will be described with reference to FIG. This embodiment is a modification of the first to fifth embodiments, and the same members or members having the same functions as those described in the first to fifth embodiments are given the same reference numerals as much as possible. Detailed description is omitted.

  Here, a modified example of the tube 202 of the tube unit 94 will be described.

  Here, the protrusions 222, 224, 226, 228 of the main body 212 of the tube 202 have an inner tube 218 formed integrally with the protrusions 222, 224, 226, 228. The projecting surfaces 222a, 224a, 226a, 228a of the projecting portions 222, 224, 226, 228 are flush with the inner peripheral surface 219a of the inner tube 218. For this reason, the projecting surfaces 222a, 224a, 226a, 228a and the inner peripheral surface 219a of the inner tube 218 cooperate to form an inner peripheral curved surface. The inner tube 218 is inside the tube body 212 and covers the outer peripheral surface 35 of the shaft 34. The inner tube 218 forms a lumen 223 between the projections 222 and 224, forms a lumen 225 between the projections 224 and 226, forms a lumen 227 between the projections 226 and 228, and between the projections 228 and 222. Lumen 229 is formed.

  The protrusions 222, 224, 226, and 228 are formed with the inner peripheral surface 213 a and the projecting surfaces 222 a, 224 a, 226 a, and 228 a of the tube main body 212 and the outer peripheral surface 219 b of the inner tube 218 with negative pressure applied to the inside of the tube main body 212. Maintain the distance between. When a negative pressure is applied between the inner side of the tube body 212 and the outer peripheral surface 219b of the inner tube 218, a pair of side surfaces 222b, 224b, 226b, 228b and a pair of side surfaces 222b, 224b, 226b, 228b, and Spaces (gap) S are formed between the pair of side surfaces 222b, 224b, 226b, 228b and the outer peripheral surface 219b of the inner tube 218 by the inner peripheral surface 213a of the tube body 212, respectively. For this reason, the space S is maintained as a suction path.

  Although several embodiments have been specifically described so far with reference to the drawings, the present invention is not limited to the above-described embodiments, and all the embodiments performed without departing from the scope of the invention are not limited thereto. Including.

According to one aspect of the present invention, a liquid delivery device for a treatment instrument that is used by being attached to a grasping portion of a treatment instrument capable of grasping a living tissue includes a port that receives a fluid, a port that receives a fluid, Among them, a cover that covers the back surface on the opposite side to the gripping surface capable of gripping the living tissue, forms a flow path continuous from the port in cooperation with the gripping portion, and receives the liquid received from the port A cover that flows out from between a cover edge adjacent to the gripping surface of the cover and an edge of the gripping surface, and a holding portion that holds the cover and the port rotating together with the gripping portion. And have.

Claims (13)

A liquid delivery device for a treatment instrument that is used by being attached to a grasping portion of a treatment instrument capable of grasping a living tissue,
A port for receiving fluid;
A cover that is continuous with the port and covers a back surface on the opposite side to a gripping surface capable of gripping the living tissue among the gripping portions, and has a flow path that continues from the port in cooperation with the gripping portion. A liquid delivery tool comprising: a cover that is formed and that allows the liquid received from the port to flow out from between the edge of the cover adjacent to the gripping surface and the edge of the gripping surface.   The liquid delivery tool according to claim 1, wherein the flow path of the cover forms a gap with the back surface of the grip portion.   The liquid feeding device according to claim 1, wherein the flow path of the cover is formed between a tip of the edge adjacent to the gripping surface and the edge of the gripping surface.   The liquid delivery tool according to claim 1, wherein the cover is formed in a substantially ¼ spherical shape.   The liquid delivery tool according to claim 1, wherein the port is formed in a half pipe shape.   The liquid delivery tool according to claim 1, wherein the port is formed in a pipe shape.   The liquid feeding tool according to claim 1, further comprising a holding portion that holds a state in which the cover and the port rotate together with the grip portion. A pair of connecting portions provided at positions adjacent to the base end of the port;
The liquid feeder according to claim 7, wherein the holding part is formed integrally with the connecting part.   The liquid feeder according to claim 7, wherein the holding portion is provided on an edge portion of the cover and is fitted to an edge portion of the gripping surface. A pair of connecting portions provided at positions adjacent to the base end of the port;
The liquid delivery device according to claim 1, further comprising a support portion that is attached to the treatment instrument and pivotally supports the pair of connection portions so as to be rotatable according to the rotation of the gripping portion.   The liquid feeder according to claim 10, wherein the support portion includes a guide portion that guides the liquid feed pipe to the port. A liquid delivery device according to claim 1;
A treatment instrument unit, wherein the liquid delivery instrument has a treatment instrument attached to a grasping portion capable of grasping a living tissue. The treatment instrument unit according to claim 12,
An energy source for supplying energy to the treatment instrument;
A fluid source;
A treatment system comprising: a liquid supply path that is disposed between the liquid supply device and the fluid source and supplies liquid from the fluid source to the liquid supply device.

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